A New Surface Charge Neutralizing Nano-Adjuvant to Potentiate Polymyxins in Killing Mcr-1 Mediated Drug-Resistant Escherichia coli.
Hyejin ChoAtanu NaskarSohee LeeSemi KimKwang-Sun KimPublished in: Pharmaceutics (2021)
Resistance to polymyxins when treating multidrug-resistant (MDR) Gram-negative bacterial infections limit therapeutic options. Here, we report the synthesis of a nickel (Ni) doped Zinc oxide (NZO) combined with black phosphorus (BP) (NZB) nanocomposite and its synergistic action with polymyxin B (PolB) against polymyxin-resistant Escherichia coli harboring mobilized colistin resistance (mcr-1) gene. NZB and PolB combination therapy expressed a specific and strong synergy against Mcr-1 expressing E. coli cells. The underlying mechanism of the synergy is the charge neutralization of the E. coli cell surface by NZB, resulting in a more feasible incorporation of PolB to E. coli. The synergistic concentration of NZB with PolB was proved biocompatible. Thus, the NZB is the first biocompatible nano-adjuvant to polymyxins against polymyxin-resistant E. coli cells, recognizing the physical status of bacteria instead of known adjuvants targeting cellular gene products. Therefore, NZB has the potential to revive polymyxins as leading last-resort antibiotics to combat polymyxin-resistant Gram-negative bacterial infections.
Keyphrases
- gram negative
- multidrug resistant
- escherichia coli
- drug resistant
- klebsiella pneumoniae
- acinetobacter baumannii
- induced apoptosis
- combination therapy
- cell surface
- cell cycle arrest
- cancer therapy
- biofilm formation
- early stage
- quantum dots
- genome wide
- physical activity
- copy number
- signaling pathway
- endoplasmic reticulum stress
- ionic liquid
- oxidative stress
- cystic fibrosis
- reduced graphene oxide
- drug release
- cell proliferation
- zika virus
- carbon nanotubes
- mass spectrometry
- climate change
- gold nanoparticles